Cough Drops Freegells Strawberry 30ct

Manufacturer
R.L. ALBERT & SON, INC
Effective date
2025-10-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:40:40

Label at a glance#

ProductCough Drops Freegells Strawberry 30ct
Active ingredientMENTHOL
Label structure8 sections

Dosage and administration

Adults and children 5 years and over dissolve 2 lozenges (one at a time) slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor children under 5 years , ask a doctor 

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

 Menthol 2.7 mg

Purpose

OTC - PURPOSE SECTION

Cough Suppressant / Oral anesthetic

Use

INDICATIONS & USAGE SECTION

Temporarily relieves:

  • cough as may occur with a cold 
  • occasional minor irritation and sore throat

Warning

WARNINGS SECTION

Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. if sore mouth symptoms do not improve in 7 days, see your dentist or doctor promptly. These symptoms may be serious.

Ask a doctor before use if you have :

  • persistent or chronic cough such as occurs with smoking, asthma, or emphysema
  • cough accompanined by excessive phlegm (mucus)

stop use and ask doctor if 

  • cough persists for more than 7 days, tends to recur, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.
  • sore throat is severe, or irritation, pain or redness lasts or worsens
  • sore mouth does not improve in 7 days

If pregnant or breast-feeding, ask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 years and over

dissolve 2 lozenges (one at a time) slowly in mouth. Repeat every 2 hours as needed or as directed by a doctor

children under 5 years , ask a doctor 

Other information

SPL UNCLASSIFIED SECTION

  • 11 calories per drop 
  • do not use if bag is torn or open 
  • Contains : Soy

Inactive ingredients

INACTIVE INGREDIENT SECTION

Beta Carotene (color), corn syrup, eucalyptus oil, honey, natural & artificial flavors, soy lecithin, sucrose and water

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
433196menthol 2.7 MG Oral LozengePSN3
433196menthol 2.7 MG Oral LozengeSCD3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83002-010-01Cough Drops Freegells Strawberry 30ct9 in 1 CARTONLOZENGE93
83002-010-01Cough Drops Freegells Strawberry 30ct30 in 1 BAGLOZENGE303

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83002-01083002-010-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-12-20full-release2026-06-01 00:47:58

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Cough Drops Freegells Strawberry 30ctMENTHOLR.L. ALBERT & SON, INCdc077c36-c403-4b83-894a-e9922e9288412025-10-08WarningsExact identifier
ndc (package): 83002-010-01
ndc (product): 83002-010
ndc11 (package): 83002001001
spl id: 40ab6a8d-de2b-ef10-e063-6294a90a6788
spl set id: dc077c36-c403-4b83-894a-e9922e928841

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.